Literature DB >> 26408953

Fibrillin microfibrils in bone physiology.

Silvia Smaldone1, Francesco Ramirez2.   

Abstract

The severe skeletal abnormalities associated with Marfan syndrome (MFS) and congenital contractural arachnodactyly (CCA) underscore the notion that fibrillin assemblies (microfibrils and elastic fibers) play a critical role in bone formation and function in spite of representing a low abundance component of skeletal matrices. Studies of MFS and CCA mice have correlated the skeletal phenotypes of these mutant animals with distinct pathophysiological mechanisms that reflect the contextual contribution of fibrillin-1 and -2 scaffolds to TGFβ and BMP signaling during bone patterning, growth and metabolism. Illustrative examples include the unique role of fibrillin-2 in regulating BMP-dependent limb patterning and the distinct impact of the two fibrillin proteins on the commitment and differentiation of marrow mesenchymal stem cells. Collectively, these findings have important implication for our understanding of the pathophysiological mechanisms that drive age- and injury-related processes of bone degeneration.
Copyright © 2015 International Society of Matrix Biology. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Autopod patterning; Bone marrow niche; Fibrillin; Marfan syndrome; Mesenchymal stem cells; Osteopenia; TGFβ and BMP signaling

Mesh:

Substances:

Year:  2015        PMID: 26408953      PMCID: PMC4808491          DOI: 10.1016/j.matbio.2015.09.004

Source DB:  PubMed          Journal:  Matrix Biol        ISSN: 0945-053X            Impact factor:   11.583


  46 in total

1.  Interdigital regulation of digit identity and homeotic transformation by modulated BMP signaling.

Authors:  R D Dahn; J F Fallon
Journal:  Science       Date:  2000-07-21       Impact factor: 47.728

2.  Differential effects of alendronate and losartan therapy on osteopenia and aortic aneurysm in mice with severe Marfan syndrome.

Authors:  Harikiran Nistala; Sui Lee-Arteaga; Luca Carta; Jason R Cook; Silvia Smaldone; Gabriella Siciliano; Aaron N Rifkin; Harry C Dietz; Daniel B Rifkin; Francesco Ramirez
Journal:  Hum Mol Genet       Date:  2010-09-24       Impact factor: 6.150

3.  Establishment of fibrillin-deficient osteoprogenitor cell lines identifies molecular abnormalities associated with extracellular matrix perturbation of osteogenic differentiation.

Authors:  Silvia Smaldone; Luca Carta; Francesco Ramirez
Journal:  Cell Tissue Res       Date:  2011-05-03       Impact factor: 5.249

4.  Dysregulation of TGF-beta activation contributes to pathogenesis in Marfan syndrome.

Authors:  Enid R Neptune; Pamela A Frischmeyer; Dan E Arking; Loretha Myers; Tracie E Bunton; Barbara Gayraud; Francesco Ramirez; Lynn Y Sakai; Harry C Dietz
Journal:  Nat Genet       Date:  2003-02-24       Impact factor: 38.330

Review 5.  Biogenesis and function of fibrillin assemblies.

Authors:  Francesco Ramirez; Lynn Y Sakai
Journal:  Cell Tissue Res       Date:  2009-06-10       Impact factor: 5.249

6.  Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes.

Authors:  B Lee; M Godfrey; E Vitale; H Hori; M G Mattei; M Sarfarazi; P Tsipouras; F Ramirez; D W Hollister
Journal:  Nature       Date:  1991-07-25       Impact factor: 49.962

7.  Abnormal muscle mechanosignaling triggers cardiomyopathy in mice with Marfan syndrome.

Authors:  Jason R Cook; Luca Carta; Ludovic Bénard; Elie R Chemaly; Emily Chiu; Satish K Rao; Thomas G Hampton; Peter Yurchenco; Kevin D Costa; Roger J Hajjar; Francesco Ramirez
Journal:  J Clin Invest       Date:  2014-02-17       Impact factor: 14.808

8.  Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils.

Authors:  H Zhang; W Hu; F Ramirez
Journal:  J Cell Biol       Date:  1995-05       Impact factor: 10.539

9.  A microfibril assembly assay identifies different mechanisms of dominance underlying Marfan syndrome, stiff skin syndrome and acromelic dysplasias.

Authors:  Sacha A Jensen; Sarah Iqbal; Alicja Bulsiewicz; Penny A Handford
Journal:  Hum Mol Genet       Date:  2015-05-15       Impact factor: 6.150

10.  Excessive transforming growth factor-β signaling is a common mechanism in osteogenesis imperfecta.

Authors:  Ingo Grafe; Tao Yang; Stefanie Alexander; Erica P Homan; Caressa Lietman; Ming Ming Jiang; Terry Bertin; Elda Munivez; Yuqing Chen; Brian Dawson; Yoshihiro Ishikawa; Mary Ann Weis; T Kuber Sampath; Catherine Ambrose; David Eyre; Hans Peter Bächinger; Brendan Lee
Journal:  Nat Med       Date:  2014-05-04       Impact factor: 53.440

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  12 in total

1.  Contribution of metabolic disease to bone fragility in MAGP1-deficient mice.

Authors:  S E Turecamo; T A Walji; T J Broekelmann; J W Williams; S Ivanov; N K Wee; J D Procknow; M R McManus; G J Randolph; E L Scheller; R P Mecham; C S Craft
Journal:  Matrix Biol       Date:  2018-03-05       Impact factor: 11.583

Review 2.  Marfan syndrome; A connective tissue disease at the crossroads of mechanotransduction, TGFβ signaling and cell stemness.

Authors:  Francesco Ramirez; Cristina Caescu; Elisabeth Wondimu; Josephine Galatioto
Journal:  Matrix Biol       Date:  2017-08-04       Impact factor: 11.583

Review 3.  Microfibril-associated glycoproteins MAGP-1 and MAGP-2 in disease.

Authors:  Clarissa S Craft; Thomas J Broekelmann; Robert P Mecham
Journal:  Matrix Biol       Date:  2018-03-07       Impact factor: 11.583

Review 4.  The extracellular matrix of hematopoietic stem cell niches.

Authors:  Cornelia Lee-Thedieck; Peter Schertl; Gerd Klein
Journal:  Adv Drug Deliv Rev       Date:  2021-11-25       Impact factor: 15.470

5.  Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family.

Authors:  Jing Chen; Qinqin Xiang; Mei Yang; Shanling Liu; Xiao Xiao; Bocheng Xu; Hanbing Xie; He Wang
Journal:  BMC Med Genomics       Date:  2022-07-08       Impact factor: 3.622

6.  A novel interaction between megakaryocytes and activated fibrocytes increases TGF-β bioavailability in the Gata1(low) mouse model of myelofibrosis.

Authors:  Maria Zingariello; Alessandra Ruggeri; Fabrizio Martelli; Manuela Marra; Laura Sancillo; Ilaria Ceglia; Rosa Alba Rana; Anna Rita Migliaccio
Journal:  Am J Blood Res       Date:  2015-12-25

Review 7.  Marfan syndrome.

Authors:  Dianna M Milewicz; Alan C Braverman; Julie De Backer; Shaine A Morris; Catherine Boileau; Irene H Maumenee; Guillaume Jondeau; Arturo Evangelista; Reed E Pyeritz
Journal:  Nat Rev Dis Primers       Date:  2021-09-02       Impact factor: 65.038

8.  Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly.

Authors:  Guoling You; Bailing Zu; Bo Wang; Zhigang Wang; Yunlan Xu; Qihua Fu
Journal:  Int J Mol Sci       Date:  2017-04-05       Impact factor: 5.923

Review 9.  Fell-Muir Lecture: Fibrillin microfibrils: structural tensometers of elastic tissues?

Authors:  Cay M Kielty
Journal:  Int J Exp Pathol       Date:  2017-09-14       Impact factor: 1.925

Review 10.  Estrogen-related mechanisms in sex differences of hypertension and target organ damage.

Authors:  Andrea Rodrigues Sabbatini; Georgios Kararigas
Journal:  Biol Sex Differ       Date:  2020-06-01       Impact factor: 5.027

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